ID
34669
Description
An 8-week Study to Evaluate the Dose Response of AHU377 in Combination With Valsartan 320 mg in Patients With Mild-to-moderate Systolic Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01281306
Link
https://clinicaltrials.gov/show/NCT01281306
Keywords
Versions (1)
- 1/22/19 1/22/19 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
January 22, 2019
DOI
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License
Creative Commons BY 4.0
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Eligibility Systolic Hypertension NCT01281306
Eligibility Systolic Hypertension NCT01281306
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Hypertension, severe
Data type
boolean
Alias
- UMLS CUI [1]
- C4013784
Description
Angioedema Drug-induced | Angioedema
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0002994
- UMLS CUI [1,2]
- C0458082
- UMLS CUI [2]
- C0002994
Description
Pregnancy | Breast Feeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
Childbearing Potential | Exception Use of Contraceptive methods
Data type
boolean
Alias
- UMLS CUI [1]
- C3831118
- UMLS CUI [2,1]
- C1705847
- UMLS CUI [2,2]
- C1524063
- UMLS CUI [2,3]
- C0700589
Description
Secondary hypertension
Data type
boolean
Alias
- UMLS CUI [1]
- C0155616
Description
Eligibility Criteria Study Protocol
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1516637
- UMLS CUI [1,2]
- C2348563
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Eligibility Systolic Hypertension NCT01281306
- StudyEvent: Eligibility
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C0332155 (UMLS CUI [4])
C0585941 (UMLS CUI [5])
C0525058 (UMLS CUI [2])
C3489773 (UMLS CUI [3,1])
C0205170 (UMLS CUI [3,2])
C0458082 (UMLS CUI [1,2])
C0002994 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
C1705847 (UMLS CUI [2,1])
C1524063 (UMLS CUI [2,2])
C0700589 (UMLS CUI [2,3])
C2348563 (UMLS CUI [1,2])